SCHEDULES

SCHEDULE 7Qualified persons

PART 3Obligations of qualified person

13

1

This paragraph applies F1in Northern Ireland where—

a

a medicinal product which has undergone the controls referred to in F2paragraph 12A in a member State is imported to Northern Ireland; and

b

each batch of the product is accompanied by control reports signed by another qualified person in respect of the medicinal product.

2

Where this paragraph applies, the qualified person is not responsible for carrying out the controls referred to in paragraph F312A.